Movement protein

TMV MP30 localizes to plasmodesmata when fused to GFP. This image was captured using confocal laser scanning microscopy

In order for a virus to infect a plant, it must spread between cells in so it can spread throughout the plant. Plant cell walls make this spread quite difficult and therefore, for this to occur, movement proteins must be present. A movement protein (MP) is a specific virus-encoded protein that is considered to be a general feature of plant genomes. They allow for local and systemic viral spread throughout a plant. MPs were first studied in the Tobacco Mosaic Virus (TMV) where it was found that viruses were unable to spread without the presence of a specific protein. In general, the plant viruses first, move within the cell from replication sites to the plasmodesmata (PD). Then, the virus is able to go through the PD and spread to other cells. This process is controlled through MPs. Different MPs use different mechanisms and pathways to regulate this spread of some viruses. Nearly all plants express at least one MP, while some can encode many different MPs which help with cell to cell viral transmission. They serve to increase the size exclusion limits (SEL) of plasmodesmata to allow for greater spread of the virus.

Plant viral movement protein regulation

Viral MPs can undergo some sort of regulation. They can be phosphorylated by plant protein kinases which can inactivate the viral MPs and provide an avenue for post-translational modification and regulation of viral movement. Phosphorylation also can assist in regulating viral infectivity. Plasmodesmata function can regulate the stability of MP-vNA complexes which are formed in order for viruses to be transported via the movement protein. Phosphorylation during the tobacco mosaic virus-MP-vRNA transport could be responsible for playing a role in regulating the degree of infectivity of the virus.

Function of movement proteins

Movement proteins can assist in unraveling key mechanisms that help control and regulate macromolecule transport within and between plant cells. MPs can use plasmodesmata, however, they are also able to alter and intercept intercellular channels based on if they are fully differentiated or if they are developing cells. When MPs are actively being expressed, the cell wall barrier to the movement of plant viruses is eliminated which can imply that movement proteins can play a role in changing cell architecture. MPs and other viral components can interact with the endomembrane system along with the cytoskeletal network right before the virus crosses the cell wall. These interactions occur in order to identify the viral genome and direct it to the cell wall for transport. Different viral encoded MPs are responsible for interfering with plasmodesmal gating. Research has suggested that there could even be plasmodesmal targeting sequences within movement proteins and that these proteins could even serve as tools to identify certain components of the plasmodesmata. There has not been extensive similarities in sequences in MPs that belong to different plant virus taxonomic groups. Additionally, some transport systems for viruses just need a single MP while others may need additional virus encoded proteins in order to facilitate the transport of viral genomes.

Mechanisms of MPs

There are multiple different mechanisms that MPs can use. The 30-kDa MP found in the TMV has been shown to alter the size exclusion limit of PD. It is also able to bind ssRNAs and also may pass through plasmodesmata as an RNP complex containing virus genomic RNA. Some MPs have the necessary protein motifs to undergo cell to cell movement without the help of other virus-specific proteins. These MPs are able to sequence non-specific RNA binding and help the movement of other viruses that are unable to transport themselves. Another type of MP mechanism involves the movement of the plasmodesmata internal structures such as the desmotubule and the transmission of entire virions, from infected cells to adjacent cells.

References

1. Koonin, E. V.; Mushegian, A. R.; Ryabov, E. V.; Dolja, V. V. (1991-12-01). "Diverse Groups of Plant RNA and DNA Viruses Share Related Movement Proteins that may Possess Chaperone-like Activity". Journal of General Virology. 72 (12): 2895–2903. doi:10.1099/0022-1317-72-12-2895. ISSN 0022-1317.
2. Taliansky, Michael; Torrance, Lesley; Kalinina, Natalia O. (2008), Foster, Gary D.; Johansen, I. Elisabeth; Hong, Yiguo; Nagy, Peter D. (eds.), "Role of Plant Virus Movement Proteins", Plant Virology Protocols, Totowa, NJ: Humana Press, vol. 451, pp. 33–54, doi:10.1007/978-1-59745-102-4_3, ISBN 978-1-58829-827-0, retrieved 2022-05-04
3. Lucas, William J. (2006). "Plant viral movement proteins: Agents for cell-to-cell trafficking of viral genomes". Virology. 344 (1): 169–184. doi:10.1016/j.virol.2005.09.026.
4. Lazarowitz, Sondra G.; Beachy, Roger N. (1999-04). "Viral Movement Proteins as Probes for Intracellular and Intercellular Trafficking in Plants". The Plant Cell. 11 (4): 535–548. doi:10.1105/tpc.11.4.535. ISSN 1040-4651. PMC 144200. PMID 10213776.
5. Lee, Jung-Youn; Lucas, William J (2001-01). "Phosphorylation of viral movement proteins – regulation of cell-to-cell trafficking". Trends in Microbiology. 9 (1): 5–8. doi:10.1016/S0966-842X(00)01901-6.
6. Morozov, Sergey Y.; Solovyev, Andrey G.; Morozov, Sergey Y.; Solovyev, Andrey G. (2020). "Small hydrophobic viral proteins involved in intercellular movement of diverse plant virus genomes". AIMS Microbiology. 6 (3): 305–329. doi:10.3934/microbiol.2020019. ISSN 2471-1888. PMC 7595835. PMID 33134746.